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Terminated Phase 2 Interventional Results available

Efficacy and Safety of AQX-1125 in Subjects With Chronic Prostatitis/Chronic Pelvic Pain Syndrome

ClinicalTrials.gov ID: NCT03500159

Public ClinicalTrials.gov record NCT03500159. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 6:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 12-Week, Randomized, Multi-Center, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Trial to Evaluate the Efficacy and Safety of AQX-1125 (200 mg) in Male Subjects With Chronic Prostatitis/Chronic Pelvic Pain Syndrome

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a randomized, multi-center, double-blind, parallel-group study, enrolling approximately 100 male subjects diagnosed with CP/CPPS to evaluate the effect of 12-week treatment with AQX-1125 (active drug) compared to placebo. The subjects will be randomized to receive orally once-daily either AQX-1125 (200 mg) or placebo in a 1:1 ratio across approximately 30 centers in North America (United States and Canada). The study will consist of a screening period of up to 3 weeks, a 12-week treatment period followed by a 4-week off drug safety follow-up period, and an ophthalmic safety follow-up call at 3 months and visit at 6 months post last dose, for a total study duration of about 41 weeks.

Study identification

NCT ID
NCT03500159
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
3 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 18, 2018 (Actual)
Primary completion
Jul 17, 2018 (Actual)
Completion
Jul 17, 2018 (Actual)
Last update posted
Jan 9, 2019

2018

United States locations

U.S. sites
23
U.S. states
17
U.S. cities
22
Facility City State ZIP Site status
Site 1026 Homewood Alabama 35209 —
Site 1010 Mobile Alabama 36608 —
Site 1004 Tucson Arizona 85710 —
Site 1028 Laguna Hills California 92653 —
Site 1018 Los Alamitos California 90720 —
Site 1016 Los Angeles California 90048 —
Site 1020 Los Angeles California 90048 —
Site 1027 New Port Richey Florida 34653 —
Site 1013 Coeur d'Alene Idaho 83814 —
Site 1015 Springfield Illinois 62769 —
Site 1023 Jeffersonville Indiana 47130 —
Site 1014 West Des Moines Iowa 50266 —
Site 1012 Shreveport Louisiana 71106 —
Site 1002 Royal Oak Michigan 48072 —
Site 1011 Albuquerque New Mexico 87109 —
Site 1009 Lake Success New York 11042 —
Site 1021 Charlotte North Carolina 28207 —
Site 1008 Raleigh North Carolina 27612 —
Site 1019 Wilmington North Carolina 28401 —
Site 1001 Cleveland Ohio 44195 —
Site 1017 Oklahoma City Oklahoma 73120 —
Site 1007 Philadelphia Pennsylvania 19140 —
Site 1022 Dallas Texas 75231 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03500159, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 9, 2019 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03500159 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →